A straightforward synthesis of aryl aziridines is reported from readily available azides and alkenes and using technical solvents in the presence of air. This methodology does not require any additives and the obtained compounds can be employed in ring opening and ring expansion reactions
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-amin...
Reaction of 2-(cyanomethyl)aziridines with N-bromosuccinimide in dichloromethane results in the form...
Ring-opening and cyclization of aziridines with aryl azides in the presence of TfOH has been develop...
The regiochemical outcome of the ring opening of the activated and unactivated title aziridines was ...
A new strategy to open the 2-allyl-2H-azirines by 1,8-diazabicyclo[5.4.0] undec-7-ene (DBU) promotio...
The ring opening reaction of N-tosyl aziridines with dilithium arylthienylcyanocuprates generated fr...
Reaction of N-tosylaziridines with nitriles and carbonyls to produce imidazolines and oxazolidines h...
The regiochemical outcome of the ring opening of aziridines bearing a polar remote functionality was...
The metal-free synthesis of 2-substituted and 2,3-disubstituted morpholines through a one-pot strate...
N-alkenyl aziridines are a unique class of molecules that do not behave as typical enamines as a res...
In the past decades aziridines have played a role of versatile intermidiates and important precursor...
3-Alkoxy-2H-azirines 4 have been prepared by treatment of enol ethers 6 with iodine azide followed b...
Multisubstituted furans were prepared from dialkyl 2-(aziridin-2-ylmethylene)malonate and/or 1,3-di...
A new strategy to open the 2-allyl-2<i>H</i>-azirines by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) p...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-amin...
Reaction of 2-(cyanomethyl)aziridines with N-bromosuccinimide in dichloromethane results in the form...
Ring-opening and cyclization of aziridines with aryl azides in the presence of TfOH has been develop...
The regiochemical outcome of the ring opening of the activated and unactivated title aziridines was ...
A new strategy to open the 2-allyl-2H-azirines by 1,8-diazabicyclo[5.4.0] undec-7-ene (DBU) promotio...
The ring opening reaction of N-tosyl aziridines with dilithium arylthienylcyanocuprates generated fr...
Reaction of N-tosylaziridines with nitriles and carbonyls to produce imidazolines and oxazolidines h...
The regiochemical outcome of the ring opening of aziridines bearing a polar remote functionality was...
The metal-free synthesis of 2-substituted and 2,3-disubstituted morpholines through a one-pot strate...
N-alkenyl aziridines are a unique class of molecules that do not behave as typical enamines as a res...
In the past decades aziridines have played a role of versatile intermidiates and important precursor...
3-Alkoxy-2H-azirines 4 have been prepared by treatment of enol ethers 6 with iodine azide followed b...
Multisubstituted furans were prepared from dialkyl 2-(aziridin-2-ylmethylene)malonate and/or 1,3-di...
A new strategy to open the 2-allyl-2<i>H</i>-azirines by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) p...
An efficient ring cleavage of aziridines with acids has been studied in the absence of any catalyst....
(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-amin...
Reaction of 2-(cyanomethyl)aziridines with N-bromosuccinimide in dichloromethane results in the form...